290315-11-6 Usage
Uses
Used in Organic Synthesis:
Tert-butyl (2R,3S)-3-(benzyloxy)-2-(3-bromo-2-oxopropyl)piperidine-1-carboxylate is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and functional groups allow for versatile chemical reactions, enabling the synthesis of a wide range of target molecules.
Used in Drug Discovery:
In the pharmaceutical industry, tert-butyl (2R,3S)-3-(benzyloxy)-2-(3-bromo-2-oxopropyl)piperidine-1-carboxylate is used as a lead compound for the development of new drugs. Its specific stereochemistry and functional groups may provide opportunities for the design of novel therapeutic agents with improved selectivity and potency.
Used in Medicinal Chemistry:
Tert-butyl (2R,3S)-3-(benzyloxy)-2-(3-bromo-2-oxopropyl)piperidine-1-carboxylate is utilized as a building block in the synthesis of complex organic molecules with potential medicinal properties. Its unique structure and functional groups can be exploited to create new chemical entities with therapeutic potential.
Used in Chemical Research:
In the field of chemical research, tert-butyl (2R,3S)-3-(benzyloxy)-2-(3-bromo-2-oxopropyl)piperidine-1-carboxylate serves as a model compound for studying the reactivity and selectivity of various chemical reactions. Its unique structure and functional groups provide insights into the underlying mechanisms of organic transformations and help to advance the understanding of chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 290315-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,1 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 290315-11:
(8*2)+(7*9)+(6*0)+(5*3)+(4*1)+(3*5)+(2*1)+(1*1)=116
116 % 10 = 6
So 290315-11-6 is a valid CAS Registry Number.
290315-11-6Relevant articles and documents
The formal synthesis of isofebrifugine using stereoselective intramolecular Michael addition
Sudhakar, Neela,Srinivasulu, Gannoju,Rao, Ganipisetti Srinivas,Rao, Batchu Venkateswara
experimental part, p. 2153 - 2158 (2009/04/05)
The formal synthesis of isofebrifugine, a bioactive alkaloid, was achieved via a stereoselective intramolecular Michael addition reaction from d-mannitol.
Catalytic asymmetric synthesis of febrifugine and isofebrifugine
Kobayashi, Shu,Ueno, Masaharu,Suzuki, Ritsu,Ishitani, Haruro
, p. 2175 - 2178 (2007/10/03)
Antimalarial alkaloids, febrifugine (1) and isofebrifugine (2), were synthesized from simple achiral starting materials using tin(II)-catalyzed catalytic asymmetric aldol reaction and lanthanide-catalyzed aqueous three- component reaction as the key steps. These unambigous total syntheses revealed that the absolute configurations of febrifugine and isofebrifugine were not (2'S, 3'R) and (2'R, 3'R) as reported previously but (2'R, 3'S) and (2'S, 3'S), respectively.
